• Title of article

    Interaction between factor V Leiden and serum LDL cholesterol increases the risk of atherosclerosis

  • Author/Authors

    Henry Volzke، نويسنده , , Birger Wolff، نويسنده , , Rita Grimm، نويسنده , , Daniel M. Robinson، نويسنده , , Gudrun Schuster، نويسنده , , Falko H. Herrmann، نويسنده , , Wolfgang Motz، نويسنده , , Rainer Rettig، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2005
  • Pages
    7
  • From page
    341
  • To page
    347
  • Abstract
    We investigated the association between the factor V Leiden gene variant and carotid atherosclerosis in a cross-sectional study and explored possible associations between this gene variant and coronary artery disease (CAD) in a case-control study. Methods: The presence (n = 1696) or absence (n = 703) of carotid atherosclerosis were sonographically assessed among participants of the population-based Study of Health in Pomerania (SHIP). The case-control study included 1021 patients with severe CAD and 2791 healthy SHIP participants. The factor V Leiden gene variant was determined by PCR and MnlI digestion. Results: Multivariable analyses revealed no independent association between the factor V Leiden gene variant per se and carotid atherosclerosis or CAD. In the cross-sectional study, there was an interaction between the factor V Leiden gene variant and serum LDL cholesterol in non-diabetics with respect to the risk of carotid atherosclerosis. In the case-control study a similar interaction was found for CAD. In both studies the atherosclerotic risk increased with rising serum LDL cholesterol concentrations in carriers of the factor V Leiden gene variant. Conclusion: The co-existence between the factor V Leiden gene variant and high serum LDL cholesterol is independently associated with the risk of atherosclerosis.
  • Keywords
    APC resistance , coronary artery disease , Ship , Factor V Leiden , atherosclerosis
  • Journal title
    Atherosclerosis
  • Serial Year
    2005
  • Journal title
    Atherosclerosis
  • Record number

    631668